# autosomal dominant non-syndromic intellectual disability 39

> autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of MYT1L on chromosome 2p25.3

**Wikidata**: [Q50349643](https://www.wikidata.org/wiki/Q50349643)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-39


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Diagnostic exome sequencing in persons with severe intellectual disability
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/32897f25-e36a-4ec8-9401-0374a95e06a5--2020-08-18T16:00:00)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_32897f25-e36a-4ec8-9401-0374a95e06a5-2020-08-18T160000.000Z)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000186487/MONDO_0014678)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)